ENST00000231749.8:c.118G=
MANE Select
|
ENSP00000231749.3:p.Glu40=
|
|
ENST00000231749.7:c.118G=
|
ENSP00000231749.3:p.Glu40=
|
|
ENST00000360165.7:c.118G=
|
ENSP00000353289.3:p.Glu40=
|
|
ENST00000431869.1:c.*8G=
|
ENSP00000391545.1:n.*8G=
|
|
ENST00000442887.1:c.-12G=
|
ENSP00000393687.1:n.-12G=
|
|
ENST00000443080.5:c.*8G=
|
ENSP00000415661.1:n.*8G=
|
|
ENST00000468182.1:n.220G=
|
|
|
NM_001308379.1:c.118G=
|
NP_001295308.1:p.Glu40=
|
|
NM_015896.2:c.118G=
|
NP_056980.2:p.Glu40=
|
|
NM_015896.3:c.118G=
|
NP_056980.2:p.Glu40=
|
|
XM_005265216.2:c.-37+281G=
|
XP_005265273.1:n.-37+281G=
|
|
XM_005265216.3:c.-37+281G=
|
XP_005265273.1:n.-37+281G=
|
|
NM_015896.4:c.118G=
MANE Select
|
NP_056980.2:p.Glu40=
|
|
NM_001308379.2:c.118G=
|
NP_001295308.1:p.Glu40=
|
|